N-(5-bromo-3-nitropyridin-2-yl)acetamide

Base Information

• Chemical Name: N-(5-bromo-3-nitropyridin-2-yl)acetamide
• CAS No.: 381679-24-9
• Molecular Formula: C₇H₆BrN₃O₃
• Molecular Weight: 260.047
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID20382678
• Wikidata: Q82174043
• Mol file: 381679-24-9.mol

Synonyms:N-(5-bromo-3-nitropyridin-2-yl)acetamide;381679-24-9;2-ACETAMIDO-5-BROMO-3-NITROPYRIDINE;DTXSID20382678;MFCD00770745;STK763396;AKOS001626651;BS-23678;CS-0083369;EU-0007022;A873912;SR-01000452655;SR-01000452655-1

Chemical Property of N-(5-bromo-3-nitropyridin-2-yl)acetamide

Chemical Property:

• Vapor Pressure: 2.22E-07mmHg at 25°C
• Melting Point: 210 °C(Solv: ethanol (64-17-5); methanol (67-56-1))
• Boiling Point: 423.5°Cat760mmHg
• PKA: 11.65±0.70(Predicted)
• Flash Point: 209.9°C
• PSA: 87.81000
• Density: 1.808g/cm³
• LogP: 2.30690
• Storage Temp.: 2-8°C
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 258.95925
• Heavy Atom Count: 14
• Complexity: 243

Purity/Quality:

99% ^*data from raw suppliers

2-Acetamido-5-bromo-3-nitropyridine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)NC1=C(C=C(C=N1)Br)[N+](=O)[O-]
• Uses: 2-Acetamido-5-bromo-3-nitropyridine is a chemical reagent used in the syntheis of ribofuranosides of substituted imidazo[c]pyridines as purine antagonists.

Technology Process of N-(5-bromo-3-nitropyridin-2-yl)acetamide

There total 1 articles about N-(5-bromo-3-nitropyridin-2-yl)acetamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

5-bromo-3-nitro-pyridin-2-ylamine (6945-68-2) + acetic acid (64-19-7,77671-22-8) → C7H6BrN3O3 (381679-24-9)

Guidance literature:

With sulfuric acid; acetic anhydride; at 60 ℃; for 2h; Inert atmosphere;

upstream raw materials:

5-bromo-3-nitro-pyridin-2-ylamine

acetic acid

Refernces